X-linked mental retardation syndrome with characteristic ?coarse? facial appearance, brachydactyly, and short stature maps to proximal Xq
- 21 June 1999
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 85 (3), 230-235
- https://doi.org/10.1002/(sici)1096-8628(19990730)85:3<230::aid-ajmg9>3.0.co;2-o
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- XLMR genes: Update 1998American Journal of Medical Genetics, 1999
- X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content.Genome Research, 1997
- A novel X–linked gene, DDP, shows mutations in families with deafness (DFN–1), dystonia, mental deficiency and blindnessNature Genetics, 1996
- Letter to the editor: Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)American Journal of Medical Genetics, 1996
- Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)Cell, 1995
- Clinical and hematologic aspects of the X‐linked α‐thalassemia/mental retardation syndrome (ATR‐X)American Journal of Medical Genetics, 1995
- Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3Human Molecular Genetics, 1994
- Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcriptsHuman Molecular Genetics, 1993
- Unique X‐linked mental retardation syndrome with fingertip arches and contractures linked to Xq21.31American Journal of Medical Genetics, 1991
- Nonspecific X‐linked mental retardation II: The frequency in British ColumbiaAmerican Journal of Medical Genetics, 1980